A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693281



Internal ID15429933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112452175..112454553hg38UCSC Ensembl
Innerchr13:113106489..113108867hg19UCSC Ensembl
Innerchr13:112154490..112156868hg18UCSC Ensembl
Innerchr13:112154490..112156868hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg382379
hg192379
hg182379
hg172379
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517711
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693281
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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